Function of oxidative stress in the regulation of hematopoietic stem cell-niche interaction

被引:104
作者
Hosokawa, Kentaro [1 ]
Arai, Fumio [1 ]
Yoshihara, Hiroki [1 ]
Nakamura, Yuka [1 ]
Gomei, Yumiko [1 ]
Iwasaki, Hiroko [1 ]
Miyamoto, Kana [1 ]
Shima, Haruko [1 ]
Ito, Keisuke [1 ]
Suda, Toshio [1 ]
机构
[1] Keio Univ, Sch Med, Sakaguchi Lab Dev Biol, Dept Cell Differentiat,Shinjuku Ku, Tokyo 1608582, Japan
关键词
hematopoietic stem cell; oxidative stress; niche; cell adhesion; N-cadherin; cell cycle;
D O I
10.1016/j.bbrc.2007.09.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During postnatal life, the bone marrow (BM) supports both self-renewal and differentiation of hematopoietic stem cells (HSCs) in specialized niches, such as osteoblastic niche and vascular niche. A cell adhesion molecule, N-cadherin expressed in the HSCs and osteoblasts, suggesting that homophylic binding of N-cadherin induce the adhesion of HSCs to the niche cells. Here we demonstrate that an anti-cancer drug, 5-fuluorouracil induces reactive oxygen species (ROS) in HSCs, which suppressed N-cadherin expression. These events result in the shift of side population (SP) cells to non-SP cells, indicating that quiescent HSCs are detached from the niche. Administration of a potent anti-oxidant, N-acetyl cystein (NAC) suppressed the shift from SP cells. These data suggest that ROS suppressed the N-cadherin-mediated cell adhesion, and induce the exit of HSCs from the niche. (C) 2007 Published by Elsevier Inc.
引用
收藏
页码:578 / 583
页数:6
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